- About this Journal ·
- Abstracting and Indexing ·
- Aims and Scope ·
- Article Processing Charges ·
- Articles in Press ·
- Author Guidelines ·
- Bibliographic Information ·
- Citations to this Journal ·
- Contact Information ·
- Editorial Board ·
- Editorial Workflow ·
- Free eTOC Alerts ·
- Publication Ethics ·
- Reviewers Acknowledgment ·
- Submit a Manuscript ·
- Subscription Information ·
- Table of Contents
International Journal of Electrochemistry
Volume 2012 (2012), Article ID 130980, 7 pages
Synthesis and Electroanalytical Performance of a Composite Material Based on Poly(3,4-ethylenedioxythiophene) Doped with Lignosulfonate
Institute of Chemistry and Technical Electrochemistry, Poznan University of Technology, Piotrowo 3, 60-965 Poznan, Poland
Received 15 June 2011; Accepted 4 October 2011
Academic Editor: Jiujun Zhang
Copyright © 2012 Grzegorz Milczarek and Tomasz Rebis. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
3,4-ethylenedioxythiophene (EDOT) was electropolymerized in the presence of sodium lignosulfonate (LS) at constant current density of 0.25 mA cm−2. As a result, a thin composite film consisting of poly(3,4-Ethylenedioxythiophene) and LS (PEDOT/LS) was deposited on the electrode surface. Unlike PEDOT, PEDOT/LS shows appreciable redox activity due to LS-derived quinone moieties with diffusion-like charge propagation across the film thickness. The film-modified gold electrodes can be used as voltammetric sensor of uric acid (UA) in the presence of ascorbic acid (AA). Interestingly, the UA response is catalysed by the presence of AA, and for high AA/UA concentration ratios more than 10-fold enhancement of the UA peak currents are apparent.
Conducting polymers (CPs) have been attracting attention of material scientists and electrochemists for many years because of their easy preparation, high electroconductivity, as well as attractive electrochemical and optical properties . Properties of CPs are to some extend a function of the counterion balancing the positive charge of the protonated conjugated polymer chains. Therefore, various sulfonated compounds have been successfully applied to dope conducting polymers and thus to tune their properties. Among those sulfonic acids , sulfonated phthalocyanines , sulfonated anthraquinone and benzoquinone derivatives [4, 5], and sulfonated polymers [6–9] are the most representative examples. On the other hand, lignosulfonates (LSs) obtainable in huge quantities as a byproduct of pulp and paper industry attracted rather little attention as dopants of CPs. For instance, Roy et al.  used lignosulfonate as polyanion to dope chemically synthesized polyaniline. Similarly LS was used as dopant for polypyrrole . Other electrochemical applications of LSs were also reported. For example, Vagin et al. electropolymerized LS on steel and showed anticorrosion properties of thus formed thin film. The same authors also studied electrochemistry of lignosulfonate on glassy carbon and reported it not to undergo electropolymerization on this electrode . Contrary to the latter observation, we electropolymerized LSs from an acidic electrolyte on preactivated glassy carbon and observed high redox activity of the formed coatings which could be practically applied in the electrocatalytic reduction of acidic nitrite  or electrocatalytic oxidation of NADH . We also proved that LSs can be used as valuable electrolyte additives in electrochemical supercapacitors .
The aim of the present work is to investigate a possibility for electrochemical polymerization of 3,4-ethylenedioxythiophene EDOT in the presence of commercially available LS into thin redox-active films. With the ease of preparation and its low costs resulting from the usage of industrial byproducts, such films exhibiting valuable electrocatalytic properties could find widespread applications in the development of electrochemical sensing platforms.
3,4-Ethylenedioxythiophene (EDOT), lignosulfonic acid (sodium salt) (Mw 52,000), lithium perchlorate trihydrate, and acetonitrile (anhydrous, 99.8%) were purchased from Aldrich. Uric acid (UA) (98%) was provided by Fluka and ascorbic acid (AA) by POCH (Gliwice, Poland).
Before its modification, the working electrode (polycrystalline gold, 1.0 mm diameter) was polished with hydrophilic silica slurries of 0.05 μm on Buehler polishing cloth with water as a lubricant, rinsed with water, and sonicated in a water bath for 5 min.
Electrodeposition of PEDOT/LS composite films was performed by the modifying procedure commonly applied for unmodified PEDOT. A solution of 1 mg cm−3 EDOT and 1 mg cm−3 LS in H2O/ACN (1/1, v/v), containing 0.1 M LiClO4 as supporting electrolyte, was used as the plating solution, and the polymerization was attained by applying a constant current density of 0.25 mA cm−2 for desired time. After modification, the PEDOT/LS-modified electrode was thoroughly rinsed with water and characterized electrochemically in phosphate buffer (pH 7.4).
All the electrochemical measurements were carried out using a μAutolab II electrochemical analyzer (EcoChemie, Utrecht-Netherlands) connected to a PC for control, data acquisition, and storage. A standard three-electrode configuration, consisting of the modified working, reference and counter electrodes, was incorporated into a glass cell (volume 20 cm3). The supporting electrolytes were degassed with a stream of purified nitrogen for 20 min. prior to the measurements. The counter electrode was a platinum wire. All potentials reported in this paper are referenced to an Ag/AgCl (3 M NaCl) electrode with no regard for the liquid junction potential.
XPS spectra of the composite film were obtained with a VSW photoelectron spectrometer (Vacuum Systems Workshop Ltd., England) using nonmonochromatized Al Kα radiation (1486.6 eV). The radiation source operated at 15 kV and 14 mA. The vacuum pressure was always kept around 3 × 10−8 mbar. The binding energy scale was corrected by referring to the aromatic peak of the C1s spectrum as being 284.6 eV.
3. Results and Discussion
3.1. Electrochemical Polymerization of EDOT in the Presence of Lignosulfonate
As we have already proven, LSs undergo strong adsorption on electrodic surfaces, and, after initial oxidation, the adsorbates show characteristic redox activity assignable to reversible oxidation reduction of quinone moieties [13, 14]. Unfortunately, the surface coverage of the redox sites was within submonolayer range. Therefore, one of the objectives of this part of the work was to optimize the composition of the deposited PEDOT/LS composite in order to force maximal activity of the LS-derived quinone groups.
Using the galvanostatic polymerization method described in experimental section, both PEDOT/ClO4 and PEDOT/LS films were obtained as adherent and continuous deposits on the Au electrode. Figure 1 shows the voltage-time tracing during polymerization in the absence and presence of LS. As seen, the presence of LS macromolecules in the PEDOT-plating solution does not cause any appreciable change in the electrode polarization voltage during the deposition. The only visible change is that in the presence of LS at the concentration of 1 mg cm−3 the voltage curve is shifted up by ca. 50 mV. It is reasonable to assume that such a small change in electrode potential in not able to change substantially the characteristics of the PEDOT polymer formed in the presence of LS compared to its LS-free counterpart.
In contrast, the cyclic voltammograms of the obtained PEDOT/ClO4 and PEDOT/LS films recorded in nearly neutral electrolyte show substantial differences (Figure 2).
The former shows typical capacitive behavior as reported for PEDOT and structurally similar polypyrrole, whereas the latter show a well-defined couple of peaks due to reaction mentioned above. This result clearly shows that the LS biomolecules are successfully incorporated into the growing PEDOT film and that their electrochemical activity is preserved. Unlike for LS alone electropolymerized on the surface coverage show much higher values being the function of LS concentration in PEDOT/LS-plating solution (Figure 3).
As seen the concentration of 1 mg cm−3 of LS provides the optimum conditions of LS incorporation into growing polymer layer judging from surface loading of quinone moieties and the fraction of redox charge contributing to the overall CV charge recorded. We also studied the effect of electrodeposition charge (time) on the two variables, and the results are presented in Figure 4. These plots show clearly that the loading of quinone moieties is nearly the linear function of the deposition charge, and, as opposite to LS polymerized on GC electrodes , the surface ladings can be tuned to reach values in the order of 10−8 mol cm−2. Besides, the efficiency of LS incorporation into the growing composite shows a peak for the polymerization charge of ca. 50 mC cm−2. Therefore, such a polymerization charge and LS concentration of 1 mg cm−3 were selected for further experiments.
3.2. XPS Analysis of the Composite Films
To give more insight into the composition of the PEDOT/LS polymer, the chemical structure of it was compared with PEDOT/ClO4 by X-ray photoelectron spectroscopy. Figure 5 shows the O(1s) and S(2p) core-level spectra for both types of polymers. The (1s) core level spectrum or PEDOT/CLO4 and PEDOT/LS are depicted in Figures 5(a) and 5(c). Significant differences can be discerned between the O(1s) signals of the two kinds of samples. The rather unimodal O(1s) peak of PEDOT/ClO4 contains the predominant feature at about 532.7 eV attributed to the oxygen atom from the PEDOT chain together with the contribution from perchlorate anions and an almost negligible band at ca. 535.3 eV. The assignment of this band is currently unknown, but most probably it is due to adsorbed water molecules. On the other hand, the oxygen band of the LS-doped composite can be deconvoluted into two signals: the predominant one at BE of ca. 532.9 assigned to ether-type oxygen atoms in EDOT units and another one at BE of 531.5 due to oxygen atoms in sulfonic groups of LS. A similar doublet was observed for PEDOT doped with polystyrene sulfonate (PSS)  or toluene sulfonate .
Basically, both PEDOT/ClO4 and PEDOT/LS spectra contain sulfur atoms of thiophene ring type manifested by a doublet of peaks at energy levels of 163.5 to 165 eV. For the former case, a minor contribution from a peak of higher binding energies is also noticed at BE of ca. 166.4 eV. Its origin may be assigned to the overoxidation of some number of thiophene rings resulting in oxygen attachment to sulfur atom . On the other hand, for the PEDOT/LS composite, the sulfur spectra shows an additional well-defined peak at higher BE (167.9 eV) due to incorporated LS molecules rich in sulfur atoms with three electronegative oxygens withdrawing the electrons from sulfur atom.
3.3. Electrochemical Characterization of the Composite Films
Figure 6 shows cyclic voltammograms recorded at various scan rates for the PEDOT/LS-modified gold electrode. As may be seen here, the voltammograms show a pair of redox peaks assignable to LS-derived quinone moieties. An analogous behavior was previously observed for LS electrodeposited on glassy carbon, but the calculated surface coverage was much lower than that observed for our composite . This can be attributed to the presence of the PEDOT network acting as an electronically conducting grid transporting the electrons between the gold support and electroactive moieties of the biopolymer. The recorded peak currents are directly related to the potential scan rate, as expected for surface-anchored redox systems. In the selected range of scan rates, the peak potentials are virtually independent of scan rate, indicating facile electron transfer kinetics.
At higher scan rates, however, the dependence of peak currents versus sweep rate becomes proportional to the square root of scan rate indication diffusion-like transport of charge within the electroactive film. We used pulsed chronoamperometry to determine the apparent charge transport diffusion coefficient, and we found that for sufficiently short times the current decay response conforms to the Cottrell equation. From this dependence, for the film polymerized at 50 mC cm−2, we found the Dct value to be 1.6 × 10−9 cm2 s−1.
3.4. Electroanalytical Application of the PEDOT/LS Composite Film
PEDOT-based materials have been reported to be a good sensing platform for the electrochemical detection of various species, especially those of biological relevance. As a model system, we chose uric acid (UA) alone and in coexistence with ascorbic acid (AA). The two compounds are commonly found in body fluids, and the monitoring of UA concentration is of clinical importance. The problem is that usually the level of UA in the sample is much lower than that of AA. Besides, on common electrodic material, for example, gold or glassy carbon, both compounds discharge anodically at similar potentials. Therefore, improvements of the sensitivity of the working electrode toward UA have been becoming a long-standing issue of electroanalyses, and PEDOT films have been suggested as those showing valuable UA/AA response ratio [18, 19].
Figure 7 summarizes our preliminary data on the application of the PEDOT/LS-modified electrodes in the electrochemical detection of UA. Regarding the reports pointing at an electrocatalytic effect of ascorbic acid on the electrochemical detection of UA on PEDOT-modified electrodes , we measured the response to UA in the absence and presence of constant concentration of AA. At unmodified gold electrode, UA and AA give broad overlapped wave at potential region of 0.2–0.6 V (not shown). In contrast, as seen in Figure 7(a), UA gives a well-defined voltammetric peak at 0.33 V at submillimolar concentration range. The presence of 1 mM AA in the background electrolyte itself does not generate any significant change in the voltammogram except that the surface redox peak of the PEDOT/LS composite is slightly enhanced. This is due to well-known catalytic activity of quinones in the mediated electrooxidation of AA . The presence of AA does not affect peak position of the coexisting UA but increases it significantly (Figure 7(b)). The observed catalytic enhancement is a function of UA concentration or the ratio between AA and UA. This dependence is plotted in Figure 8. As seen, for low UA concentrations, the catalytic effect of AA may lead to over 10-fold enhancement of the UA peak current. Note that for the PEDOT/ClO4 the effect is much less pronounced nor so much dependant on UA concentration. Even lower current enhancement was noticed for PEDOT polymerized in an organic medium; that is, 1 mM AA caused the increased in the UA response from 77.5 to 86.2 mA mM−1 cm−2 .
Electrodeposition of PEDOT in the presence of lignosulfonate has proved to give a redox active composite with quinone moieties. Electrode modification with such a composite film is a way to elaborate a voltammetric sensor for the assay of UA in the presence of coexisting AA. Interestingly, AA is found to enhance the response of UA on the PEDOT/LS film to a much stronger extent than on the LS-free PEDOT. Works are in progress to evaluate the performance of the proposed composite toward electrochemical sensing of other biomolecules.
This work was financially supported by the Polish Ministry of Science and Higher Education under project no. N N209 450939.
- T. A. Skotheim, R. L. Elsenbaumer, and J. R. Reynolds, Eds., Handbook of Conducting Polymers, Marcel Dekker, New York, NY, USA, 2nd edition, 1998.
- G. Milczarek, “Electrochemical modification of poly-aniline films in the presence of guaiacol-sulfonic acid,” Electrochemistry Communications, vol. 9, no. 1, pp. 123–127, 2007.
- G. Milczarek, “Self-doped polyaniline films prepared by electropolymerization in the presence of sulfonated nickel phthalocyanine,” Thin Solid Films, vol. 517, no. 21, pp. 6100–6104, 2009.
- X. Lang, Q. Wan, C. Feng et al., “The role of anthraquinone sulfonate dopants in promoting performance of polypyrrole composites as pseudo-capacitive electrode materials,” Synthetic Metals, vol. 160, no. 15-16, pp. 1800–1804, 2010.
- N. Oyama, T. Sarukawa, Y. Mochizuki, T. Shimomura, and S. Yamaguchi, “Significant effects of poly(3,4-ethylenedioxythiophene) additive on redox responses of poly(2,5-dihydroxy-1,4-benzoquinone-3,6-methylene) cathode for rechargeable Li batteries,” Journal of Power Sources, vol. 189, no. 1, pp. 230–239, 2009.
- J. Yan, C. Sun, F. Tan et al., “Electropolymerized poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) film on ITO glass and its application in photovoltaic device,” Solar Energy Materials and Solar Cells, vol. 94, no. 2, pp. 390–394, 2010.
- C. Y. Li, T. C. Wen, and T. F. Guo, “Sulfonated poly(diphenylamine) as a novel hole-collecting layer in polymer photovoltaic cells,” Journal of Materials Chemistry, vol. 18, no. 37, pp. 4478–4482, 2008.
- Z. Mousavi, T. Alaviuhkola, J. Bobacka, R. M. Latonen, J. Pursiainen, and A. Ivaska, “Electrochemical characterization of poly(3,4-ethylenedioxythiophene) (PEDOT) doped with sulfonated thiophenes,” Electrochimica Acta, vol. 53, no. 11, pp. 3755–3762, 2008.
- T. Kim, J. Kim, Y. Kim, T. Lee, W. Kim, and K. S. Suh, “Preparation and characterization of poly(3,4-ethylenedioxythiophene) (PEDOT) using partially sulfonated poly(styrene-butadiene-styrene) triblock copolymer as a polyelectrolyte,” Current Applied Physics, vol. 9, no. 1, pp. 120–125, 2009.
- S. Roy, J. M. Fortier, R. Nagarajan et al., “Biomimetic synthesis of a water soluble conducting molecular complex of polyaniline and lignosulfonate,” Biomacromolecules, vol. 3, no. 5, pp. 937–941, 2002.
- C. Yang and P. Liu, “Water-dispersed conductive polypyrroles doped with lignosulfonate and the weak temperature dependence of electrical conductivity,” Industrial and Engineering Chemistry Research, vol. 48, no. 21, pp. 9498–9503, 2009.
- M. Y. Vagin, S. A. Trashin, and A. A. Karyakin, “Corrosion protection of steel by electropolymerized lignins,” Electrochemistry Communications, vol. 8, no. 1, pp. 60–64, 2006.
- G. Milczarek, “Lignosulfonate-modified electrode for electrocatalytic reduction of acidic nitrite,” Electroanalysis, vol. 20, no. 2, pp. 211–214, 2008.
- G. Milczarek, “Lignosulfonate-modified electrodes: electrochemical properties and electrocatalysis of NADH oxidation,” Langmuir, vol. 25, no. 17, pp. 10345–10353, 2009.
- G. Lota and G. Milczarek, “The effect of lignosulfonates as electrolyte additives on the electrochemical performance of supercapacitors,” Electrochemistry Communications, vol. 13, no. 5, pp. 470–473, 2011.
- F. Petraki, S. Kennou, S. Nespurek, and M. Biler, “A spectroscopic study for the application of a PEDOT-type material as buffer layer in electronic devices,” Organic Electronics: Physics, Materials, Applications, vol. 11, no. 8, pp. 1423–1431, 2010.
- P. Tehrani, A. Kanciurzewska, X. Crispin, N. D. Robinson, M. Fahlman, and M. Berggren, “The effect of pH on the electrochemical over-oxidation in PEDOT:PSS films,” Solid State Ionics, vol. 177, no. 39-40, pp. 3521–3527, 2007.
- S. S. Kumar, J. Mathiyarasu, K. L. Phani, Y. K. Jain, and V. Yegnaraman, “Determination of uric acid in the presence of ascorbic acid using poly(3,4-ethylenedioxythiophene)-modified electrodes,” Electroanalysis, vol. 17, no. 24, pp. 2281–2286, 2005.
- F. Sekli-Belaidi, P. Temple-Boyer, and P. Gros, “Voltammetric microsensor using PEDOT-modified gold electrode for the simultaneous assay of ascorbic and uric acids,” Journal of Electroanalytical Chemistry, vol. 647, no. 2, pp. 159–168, 2010.
- F. Sekli-Belaidi, D. Evrard, and P. Gros, “Evidence of an EC' mechanism occurring during the simultaneous assay of ascorbic and uric acids on poly(3,4-ethylenedioxythiophene) modified gold microsensor,” Electrochemistry Communications, vol. 13, no. 5, pp. 423–425, 2011.